Inborn errors of ketogenesis and ketone body utilization.
about
A structural mapping of mutations causing succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency.Ketone body metabolism and its defects.Heterozygous Monocarboxylate Transporter 1 (MCT1, SLC16A1) Deficiency as a Cause of Recurrent Ketoacidosis.A Cause of Permanent Ketosis: GLUT-1 Deficiency.Ketone body metabolismSynthesis of Ketone BodiesUtilization of Ketone Bodies
P2860
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Inborn errors of ketogenesis and ketone body utilization.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 09 April 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Inborn errors of ketogenesis and ketone body utilization.
@en
Inborn errors of ketogenesis and ketone body utilization.
@nl
type
label
Inborn errors of ketogenesis and ketone body utilization.
@en
Inborn errors of ketogenesis and ketone body utilization.
@nl
prefLabel
Inborn errors of ketogenesis and ketone body utilization.
@en
Inborn errors of ketogenesis and ketone body utilization.
@nl
P2860
P1476
Inborn errors of ketogenesis and ketone body utilization.
@en
P2093
Jörn Oliver Sass
P2860
P2888
P356
10.1007/S10545-011-9324-6
P577
2011-04-09T00:00:00Z